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This allele, from project TCPR0416, was generated at The Centre for Phenogenomics by injecting Cas9 mRNA and four guide RNAs with spacer sequences GTGGTCGAATCCACAGCCAA, GTTGCACACCCTGATGAATA, GCATGCATGGTCGTGCCTGT and TTGAGCACGAGCACACCCAC. This resulted in a 858-bp deletion in Chr13 from 73940000 to 73940857 (GRCm38). (J:237616)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
Phenotypes
Legend：
hm: homozygous
ht: heterozygous
cn: conditional genotype
cx: complex: > 1 genome feature
tg: involves transgenes
ot: other: hemizygous, indeterminate,...
(F): Female
(M): Male
phenotype observed
N: normal phenotype
(#): related diseases count
Phenotypes：
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References Literature
Title
PMID
Journal
Year
IF
